Specialty in injectable lifesaving products including a range of pre and post surgical medications, antibiotics and anti- inflammatory products.
Various Dosage forms like Injectable cartidges, vials and disposable pen device.
Vacancy details:
- Department: IPQA- Officer
- Qualification: B.Pharma in Pharmacy
- Experience:2 – 4 years
- Salary:2.25-3.5 Lacs P.A.
Job Description : Greeting from M.J.Biopharm Pvt .Ltd!!!!
Important Details :
- Location: Mumbai (All Areas)
- Post of date:01/06/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
Job description
Role & responsibilities – IPQA Officer
The IPQA Specialist in the pharmaceutical formulation industry is responsible for ensuring that all manufacturing processes comply with standard operating procedures (SOPs), Good Manufacturing Practices (GMP), and regulatory requirements. This role involves close monitoring of production activities, documentation review, and real-time problem-solving to maintain product quality and integrity.
Key Responsibilities:
- In-Process Monitoring:
- Perform routine checks and monitoring of production processes to ensure compliance with SOPs and GMP.
- Verify the correct set-up and operation of equipment and machinery.
- Ensure that raw materials, in-process materials, and finished products meet specified quality standards.
- Documentation and Record Keeping:
- Maintain accurate and detailed records of production processes, deviations, and corrective actions.
- Review batch records and logbooks to ensure completeness and accuracy.
- Assist in the preparation of reports and documentation for regulatory inspections and audits.
- Quality Control:
- Conduct in-process sampling and testing of products to ensure compliance with quality standards.
- Evaluate test results and identify any deviations from established specifications.
- Implement corrective and preventive actions (CAPA) for any identified non-conformances.
- Compliance and Audits:
- Ensure adherence to GMP, regulatory requirements, and company policies during production activities.
- Participate in internal and external audits, providing necessary documentation and support.
- Conduct routine inspections and audits of the manufacturing area to ensure a state of continuous compliance.
- Training and Development:
- Train production staff on quality standards, SOPs, and GMP requirements.
- Stay updated on industry trends, regulatory changes, and advancements in quality assurance practices.
- Participate in continuous improvement initiatives to enhance product quality and process efficiency.
Preferred candidate profile
Must have worked for Sterile Injectable Formulation
Interested application can send CV on [email protected] or contact on 9619744167.
